Manager, Clinical Monitoring (English and French speaking) [MG713]

Precision For Medicine; Toledo; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Manager, Clinical Monitoring for its European team. This role, which can be fully remote from the UK or Spain, involves managing Clinical Research Associates to ensure high-quality clinical trials, particularly in oncology. Candidates should possess a degree in a scientific field, be fluent in English and French, and have 7+ years in clinical operations. The position emphasizes leadership, project oversight, and employee development. Competitive compensation package offered.

Formación

• Minimum 7 years in clinical operations or data management.
• At least 5 years onsite monitoring experience, particularly in oncology trials.
• 3-5 years of supervisory experience managing CRAs.

Responsabilidades

• Manage and develop the Clinical Research Associate workforce.
• Provide strategic oversight and project resourcing.
• Conduct mentoring and site visits for risk management.

Conocimientos

Leadership and people management

Fluency in English and French

Organizational skills

Problem-solving skills

Communication skills

Educación

Graduate or postgraduate degree in scientific or healthcare discipline

Herramientas

Proficiency with EMRs and EDCs

Descripción del empleo

Precision for Medicine is growing! We are hiring a Manager, Clinical Monitoring to join our European team. The position can be fully remote from the UK or Spain.

Position Summary

The Manager, Clinical Monitoring (GCM) offers an advanced development path for clinical research professionals. Responsibilities include managing and developing the organization’s Clinical Research Associate (CRA) workforce and supporting departmental initiatives to enhance quality and productivity. The role requires independent leadership, management, and motivation of a team of CRAs (employees and/or consultants) to uphold Precision for Medicine’s standards of quality.

Key focus areas include resource allocation, career development, and minimizing turnover to ensure high employee satisfaction. Essential functions include strategic oversight, project resourcing, tracking, collaboration with clinical teams, mentoring, site visits, risk management, and process improvements.

Qualifications

• Graduate or postgraduate degree, ideally in a scientific or healthcare discipline
• Fluent in English and French
• Minimum 7 years in clinical operations, data management, or related fields, with at least 5 years onsite monitoring experience, particularly in oncology trials
• 3-5 years of supervisory experience managing CRAs, including developing training and evaluation processes
• Willingness to travel domestically and internationally (~25%)

Skills and Competencies

• Mastery of ICH-GCP, local regulations, SOPs, and clinical study phases
• Strong leadership and people management skills, with high emotional intelligence
• Ability to develop training plans, work independently, and motivate teams
• Excellent organizational, problem-solving, and communication skills
• Proficiency with EMRs and EDCs

Additional information about data privacy and equal opportunity employment is included in the original description. The role involves representing Precision for Medicine professionally and adhering to company policies.